摘要

The prevalence of p53 gene mutations in many human tumors implies that p53 protein plays an important role in preventing cancers. Central among the activities ascribed to p53 is its ability to stimulate transcription of other genes that inhibit cells from entering S phase with damaged DNA. Human p53 can be studied in yeast where genetic tools can be used to identify proteins that affect its ability to stimulate transcription. Although p53 strongly stimulated reporter gene expression in wild type yeast, it only weakly stimulated reporter gene expression in Delta trr1 yeast that lacked the gene encoding thioredoxin reductase. Furthermore, ectoptic expression of TRR1 in Delta trr1 yeast restored p53-dependent reporter gene activity to high levels. Immunoblot assays established that the Delta trr1 mutation affected the activity and not the level of p53 protein, The results suggest that p53 can form disulfides and that these disulfides must be reduced in order for the protein to function as a transcription factor.

  • 出版日期1998-3-6